A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2893103



Internal ID15596230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172174428..172175404hg38UCSC Ensembl
Innerchr3:171892218..171893194hg19UCSC Ensembl
Innerchr3:173374912..173375888hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38977
hg19977
hg18977
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514998
Supporting Variants
SamplesNA07348
Known GenesFNDC3B
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2893103
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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